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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70578Generated: October 31, 2026

Benzyl Bromide → 1-(Benzylsulfonyl)-4-bromo-2-chlorobenzene

https://huagongshe.com/reaction/70578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium SulfiteHCID 24437—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-2-chlorobenzenesulfonyl chlorideHCID 2734766—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
Product1-(Benzylsulfonyl)-4-bromo-2-chlorobenzeneHCID 5845254694%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 4-bromo-2-chlorobenzenesulfonyl chloride (1.16 g), sodium sulfite (1.01 g) and sodium bicarbonate (672 mg) in water (8 mL) was stirred at 100° C. for 1.5 hours. The reaction solution was cooled to 50° C. and tetrabutylammonium bromide (1.29 g) and benzyl bromide (1.43 mL) were added, after which the mixture was stirred at 70° C. for further three hours. The reaction solution was cooled to room temperature and water was added, followed by extraction with chloroform. The organic layer was dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1) to give the title compound as a white solid (1.29 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822503B2
Source datasetuspto-grants-2014_09
ORD IDord-79a6fae59ea343e4a8161c43b77776bf
Source noteuspto-grants-2014_09